Zerkaoui Nouha
Université Mohammed V Souissi, Service d'Ophtalmologie A de l'Hôpital des Spécialités de Rabat, Centre Hospitalier Universitaire Rabat, Maroc.
Pan Afr Med J. 2018 May 2;30:1. doi: 10.11604/pamj.2018.30.1.14505. eCollection 2018.
Congenital ocular colobomas are due to incomplete closure of the fetal fissure during organogenesis. Ocular involvement can be variable ranging from a simple hole in the iris to a more severe involvement of the posterior pole (coloboma of the optic nerve, of the choroid, of the retina). We here report the case of a typical isolated bilateral iris coloboma. The study involved a 55-year old woman who discovered a typical inferonasal iris coloboma without involvement of the crystalline or of the posterior pole on ophthalmologic examination.
先天性眼裂缺损是由于器官形成期胎儿裂孔未完全闭合所致。眼部受累情况各异,从虹膜上的一个简单孔洞到后极部更严重的受累(视神经、脉络膜、视网膜裂孔)。我们在此报告一例典型的孤立性双侧虹膜裂孔缺损病例。该研究涉及一名55岁女性,她在眼科检查中发现典型的鼻下虹膜裂孔缺损,晶状体和后极部未受累。